Emil Lindbäck
University of Copenhagen
12 Papers
41 Citations
Emil Lindbäck is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 6, co-authored 8 publications.
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Papers
An isofagomine analogue with an amidine at the pseudoanomeric position.
TL;DR: (3R,4R,5R)-2-Imino-3,4-dihydroxy-5-hydroxymethylpiperidine hydrocloride or isofagomidine was synthesized from D-arabinose in 12 steps and an overall yield of 9.9%.
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The Grignard Reaction of Cyclodextrin-6-aldehydes Revisited: A Study of the Stereoselectivity Upon Addition of Organometallic Reagents to Aldehydes and Ketones
TL;DR: In this article, the secondary alcohols were treated with aromatic and aliphatic Grignard reagents to give diastereomeric mixtures of the primary alcohols with remarkable difference in polarity.
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Synthesis of Cyclodextrins with Carboxylic Acids at the Secondary Rim and an Evaluation of Their Properties as Chemzymes for Glycoside Hydrolysis
TL;DR: In this article, seven β-cyclodextrin-mono-, -di- or -tetra-O-acetic acids were investigated for their properties as catalysts of the hydrolysis of four nitrophenyl glycosides.
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A hybrid of 1-deoxynojirimycin and benzotriazole induces preferential inhibition of butyrylcholinesterase (BuChE) over acetylcholinesterase (AChE)
Tereza Cristina Santos Evangelista,Óscar López,Adrián Puerta,Miguel X. Fernandes,Sabrina Baptista Ferreira,José M. Padrón,Juan Fernández-Bolaños,Magne O. Sydnes,Emil Lindbäck +8 more
TL;DR: Four heterodimers in which the copper(I)-catalysed azide-alkyne cycloaddition was employed to connect a 1-deoxynojirimycin moiety with a benzotriazole scaffold showed preferential inhibition of BuChE over AChE in the micromolar concentration range (IC50 = 7–50‵M).
9
Two Diastereomeric Artificial Enzymes with Different Catalytic Activity
TL;DR: In this paper, two epimeric cyclodextrin-6-C-aldehydes were synthesized in 10 steps from β-cyclodexxtrin, which involved protection/partial deprotection, oxidation to a 6aldehyde, olefination, dihydroxylation, selective protection of the secondary alcohol and oxidation.
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